The Department of Laboratory Medicine and Pathology, Center for Immunology, University of Minnesota, Minneapolis, United States.
Elife. 2018 Aug 13;7:e34793. doi: 10.7554/eLife.34793.
The precise steps of iNKT subset differentiation in the thymus and periphery have been controversial. We demonstrate here that the small proportion of thymic iNKT and mucosal associated invariant T cells that express CCR7 represent a multi-potent progenitor pool that gives rise to effector subsets within the thymus. Using intra-thymic labeling, we also showed that CCR7 iNKT cells emigrate from the thymus in a dependent manner, and undergo further maturation after reaching the periphery. deficiency impaired differentiation of iNKT effector subsets and localization to the medulla. Parabiosis and intra-thymic transfer showed that thymic NKT1 and NKT17 were resident-they were not derived from and did not contribute to the peripheral pool. Finally, each thymic iNKT effector subset produces distinct factors that influence T cell development. Our findings demonstrate how the thymus is both a source of iNKT progenitors and a unique site of tissue dependent effector cell differentiation.
NKT 亚群在胸腺和外周中的分化的确切步骤一直存在争议。我们在这里证明,表达 CCR7 的胸腺和黏膜相关不变 T 细胞中的一小部分 NKT 细胞代表了一个多能祖细胞池,可在外周中产生效应子亚群。通过胸腺内标记,我们还表明 CCR7+iNKT 细胞依赖于 依赖性从胸腺中迁出,并在到达外周后进一步成熟。缺陷可损害 iNKT 效应子亚群的分化和向皮质的定位。联体共生和胸腺内转移表明,胸腺中的 NKT1 和 NKT17 是驻留的——它们不是来自于外周池,也不对外周池做出贡献。最后,每个胸腺内的 iNKT 效应子亚群都会产生影响 T 细胞发育的独特因子。我们的研究结果表明,胸腺既是 NKT 祖细胞的来源,也是组织依赖的效应细胞分化的独特部位。